نتایج جستجو برای: hereditary hearing impairment

تعداد نتایج: 288337  

2013
Jennifer J Lentz Francine M Jodelka Anthony J Hinrich Kate E McCaffrey Hamilton E Farris Matthew J Spalitta Nicolas G Bazan Dominik M Duelli Frank Rigo Michelle L Hastings

Hearing impairment is the most common sensory disorder, with congenital hearing impairment present in approximately 1 in 1,000 newborns1. Hereditary deafness is often mediated by the improper development or degeneration of cochlear hair cells2. Until now, it was not known whether such congenital failures could be mitigated by therapeutic intervention3–5. Here we show that hearing and vestibular...

Journal: :journal of rehabilitation sciences and research 0
maryam jalalipour majid soltani mehri safari colleague of fars cochlear implant center reyhane montazeri hakimeh sadeghikhah

background: reading is known as one of the most important learning tools. research results consistently have shown that even a mild hearing impairment could affect the reading skills. due to the reported differences in reading comprehension skills between hearing impaired students and their normal hearing peers, this research was conducted to compare the differences between the two groups. the ...

Ahmadshah Farhat, Ashraf Mohammadzadeh, Habibollah Esmaeli, Ne'matollah Mokhtari, Ra'na Amiri,

 Abstract  Background: Low birth weight neonates are confronted with some problems after  birth, they should be followed up and evaluated at different ages of life.The aim of this study was to determine the impact of birth weight on the risk of sensorineural hearing impairment on children.  Method: This cross sectional and retrospective study determined the prevalence  of hearing problems in lo...

Journal: :medical journal of islamic republic of iran 0
ashraf mohammadzadeh neonatal research center, mashhad university of medical science, nicu of emamrezaسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)سازمان های دیگر: neonatal research center ne'matollah mokhtari ent research center, mashhad university of medical science, ghaem hospital.iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)سازمان های دیگر: ent research center ahmadshah farhat neonatal research center, mashhad university of medical science, nicu of emamreza hospital.iran.سازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)سازمان های دیگر: neonatal research center ra'na amiri neonatal research center, mashhad university of medical science, nursing and midwifery facultyسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)سازمان های دیگر: neonatal research center habibollah esmaeli neonatal research center, mashhad university of medical science, community medicine and publicسازمان اصلی تایید شده: دانشگاه علوم پزشکی مشهد (mashhad university of medical sciences)سازمان های دیگر: neonatal research center

abstract  background: low birth weight neonates are confronted with some problems after  birth, they should be followed up and evaluated at different ages of life.the aim of this study was to determine the impact of birth weight on the risk of sensorineural hearing impairment on children.  method: this cross sectional and retrospective study determined the prevalence  of hearing problems in low...

Journal: :iranian journal of basic medical sciences 0
masoumeh falah department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran massoud houshmand national institute for genetic engineering and biotechnology, tehran, iran susan akbaroghli tehran welfare organization, tehran, iran saeid mahmodian department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran yaser ghavami department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran mohammad farhadi department and research center of ent & head and neck surgery of tehran university of medical sciences, tehran, iran

objective(s) despite the enormous heterogeneity of genetic hearing loss, most non-syndromic hearing losses are caused by mutations in the gjb2 gene. we aimed to characterize the mutation profiles of 100 iranian deaf patients that were under 10 years old. materials and methods patients were tested with direct sequencing of entire coding region of the gjb2 gene. results eight known mutations plus...

Mashallah Aghilinejad, MirSaeed Attarchi, Saber Mohammadi, Yasser Labbafinejad,

  Abstract   Background : Noise is the most common hazard in the workplace and noise induced   hearing loss considered to be the most common occupational disease as well.   Cigarette smoking, in some studies, has been known to induce hearing loss. The purpose   of this study was to evaluate the effect of contemporary exposure to occupational   noise and cigarette smoking on hearing.   Methods :...

Journal: :iranian journal of public health 0
hye-jin kwon dept. of nursing, red cross college of nursing, chung-ang university, seoul, republic of korea. ji-su kim dept. of nursing, red cross college of nursing, chung-ang university, seoul, republic of korea. yoon-jung kim dept. of nursing, red cross college of nursing, chung-ang university, seoul, republic of korea. su-jin kwon dept. of nursing, red cross college of nursing, chung-ang university, seoul, republic of korea. jin-na yu the graduate school, chung-ang university, seoul, republic of korea.

background : sensory impairment is a common condition that exerts negative effects on health-related quality of life (hrqol) in the elderly. this study aimed to determine the relationship between sensory impairment and hrqol and identify sensory-specific differences in the hrqol of elderly. methods : this study used data from the korean national health and nutrition examination survey v (2010-2...

Journal: :Children (Basel) 2023

Background: Congenital cytomegalovirus (cCMV) infection is the leading cause of non-hereditary sensorineural hearing loss in children. While about 10% children reportedly display symptoms at birth, 85–90% cCMV cases are asymptomatic. However, 10–15% these asymptomatic infants may later develop hearing, visual, or neurodevelopmental impairments. This study aimed to evaluate impact on newborns’ f...

Journal: :Health Sciences 2023

Alport syndrome (AS) is a hereditary disease that causes hearing impairment, kidney failure, and ocular abnor­malities. Because AS rare disease, it might remain undetected, meaning impacted individuals their kin have low chances of being screened receiving timely genetic counseling. Also, diagnosing requires high expertise complex technology, which are expensive for most patients. These limitat...

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